Pharmaceutical Intermediate Palmitoylethanolamide Raw Powder Material Palmitoylethanolamide Purity Palmitoylethanolamide

• Customization: Available
• Powder: Powder
• Customized: Customized
• Model NO.: D-sung Palmitoylethanolamide
• Certification: GMP, HSE, ISO 9001, USP, BP
• Suitable for: Elderly, Adult
• State: Powder
• Purity: >99%
• Product Name: Palmitoylethanolamide
• Name: Palmitoylethanolamide Powder
• Appearance: White Powde
• Color: White
• Specific: COA
• Grade: Pharmaceutical Grade
• Assay: 99%
• Application: Pharmaceutical
• Test Method: HPLC Tlc
• CAS: 544-31-0
• Mf: C18h37no2
• MW: 299.49
• Melting Point: 97-98
• Boiling Point: 461.5
• Shelf Life: 2 Years
• Transport Package: Negotiable
• Specification: 99%
• Trademark: D-sung
• Origin: Shaanxi Xi′an
• Production Capacity: 1000kg/Month

Product Description

Pharmaceutical Intermediate Palmitoylethanolamide Raw Powder Material Palmitoylethanolamide Purity Palmitoylethanolamide

Product Description

Product Details

 

Product Name	Palmitoylethanolamide
CAS NO.	544-31-0
Purity	99%
Density	0.91
Appearance and shape	White powder

Palmitoylethanolamide(pea) Powder is an endogenous fatty acid amide, belonging to the class of nuclear factor agonists.
PEA has been demonstrated to bind to a receptor in the cell-nucleus (a nuclear receptor) and exerts a great variety of biological functions related to chronic pain and inflammation. The main target is thought to be the peroxisome proliferator-activated receptor alpha (PPAR-α).

Application&Function

Function
PEA has been shown to have anti-inflammatory, anti-sensory injury, neuroprotective, and anti-convulsive properties. PEA has been exploring various pain states in people in different clinical trials for inflammation and pain syndromes.
Application
Hexadecamide ethanol is an organic synthesis intermediate and a pharmaceutical intermediate, which can be used in laboratory research and development as well as in chemical and pharmaceutical research and development.

Specification